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TCCACAGCACAGCATTCTCCTAGAG[C/T]GGGCAGGCTGGAATCCACAGGACTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604090 | ||||||||||||||||||||
Literature Links: |
DLG5 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
DLG5 - discs large MAGUK scaffold protein 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004747.3 | 4767 | Silent Mutation | CCC,CCT | P,P 1918 | NP_004738.3 | |
XM_005270276.4 | 4767 | Silent Mutation | CCC,CCT | P,P 1914 | XP_005270333.1 | |
XM_006718056.3 | 4767 | Silent Mutation | CCC,CCT | P,P 1578 | XP_006718119.1 | |
XM_006718057.3 | 4767 | Intron | XP_006718120.1 | |||
XM_011540341.2 | 4767 | Silent Mutation | CCC,CCT | P,P 1859 | XP_011538643.1 | |
XM_011540342.1 | 4767 | Silent Mutation | CCC,CCT | P,P 1828 | XP_011538644.1 | |
XM_011540344.2 | 4767 | Silent Mutation | CCC,CCT | P,P 1806 | XP_011538646.1 | |
XM_011540345.1 | 4767 | Silent Mutation | CCC,CCT | P,P 1763 | XP_011538647.1 | |
XM_011540346.2 | 4767 | Intron | XP_011538648.1 | |||
XM_011540347.2 | 4767 | Silent Mutation | CCC,CCT | P,P 1612 | XP_011538649.1 | |
XM_017016913.1 | 4767 | Silent Mutation | CCC,CCT | P,P 1824 | XP_016872402.1 | |
XM_017016914.1 | 4767 | Silent Mutation | CCC,CCT | P,P 1808 | XP_016872403.1 | |
XM_017016915.1 | 4767 | Silent Mutation | CCC,CCT | P,P 1612 | XP_016872404.1 |